Singleton J D, West S G, Reddy V V, Rak K M
Department of Medicine, Fitzsimons Army Medical Center, Aurora, CO 80045-5001, USA.
South Med J. 1995 Apr;88(4):470-4. doi: 10.1097/00007611-199504000-00019.
Central nervous system vasculitis is a rarely described complication of rheumatoid arthritis. We report a case of cerebral vasculitis in a 55-year-old woman with a 7-year history of seropositive, nodular rheumatoid arthritis. Striking multifocal abnormalities of the white matter on magnetic resonance imaging led to a suspicion of vasculitis despite lack of clinical evidence of extracranial vasculitis and normal findings on cerebrospinal fluid studies and cerebral angiography. After institution of treatment with glucocorticoids and azathioprine, she survived in stable condition for 14 months from the onset of symptoms. Postmortem examination of the brain revealed vasculitis and chronic ischemic changes.
中枢神经系统血管炎是类风湿关节炎一种鲜有描述的并发症。我们报告一例55岁女性的脑血管炎病例,该患者有7年血清学阳性、结节性类风湿关节炎病史。尽管缺乏颅外血管炎的临床证据,且脑脊液检查和脑血管造影结果正常,但磁共振成像显示白质有明显的多灶性异常,这引发了血管炎的怀疑。在使用糖皮质激素和硫唑嘌呤治疗后,她从症状出现起存活了14个月,病情稳定。脑部尸检显示有血管炎和慢性缺血性改变。